rs762065937
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs762065937(C;T) |
| Make rs762065937(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 2 |
| Position | 215064204 |
| Gene | ABCA12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs762065937 |
| dbSNP (classic) | rs762065937 |
| ClinGen | rs762065937 |
| ebi | rs762065937 |
| HLI | rs762065937 |
| Exac | rs762065937 |
| Gnomad | rs762065937 |
| Varsome | rs762065937 |
| LitVar | rs762065937 |
| Map | rs762065937 |
| PheGenI | rs762065937 |
| Biobank | rs762065937 |
| 1000 genomes | rs762065937 |
| hgdp | rs762065937 |
| ensembl | rs762065937 |
| geneview | rs762065937 |
| scholar | rs762065937 |
| rs762065937 | |
| pharmgkb | rs762065937 |
| gwascentral | rs762065937 |
| openSNP | rs762065937 |
| 23andMe | rs762065937 |
| SNPshot | rs762065937 |
| SNPdbe | rs762065937 |
| MSV3d | rs762065937 |
| GWAS Ctlg | rs762065937 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs762065937(G;G) rs762065937(T;T) |
| Alt | rs762065937(G;G) rs762065937(T;T) |
| Reference | Rs762065937(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ABCA12 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.215928927C>G |
| CLNSRC | |
| CLNACC | RCV000256128.1, |
